I‘ve learned that it’s important to be selective and rely on only certain websites for factual information about your disease(s) and medications/supplements.
Even if you don't know someone in your city with your particular disease, you are not alone in your struggles. Reach out and find someone online to help you through this.
I recently learned of this organization during the pandemic. Their emails have been very informative.
The Lupus Foundation of America will keep you updated with the latest research and clinical trials for treatments. Also, check out Lupus Corner: https://lupuscorner.com
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